Ebstein's anomaly is a rare congenital heart defect that affects the structure and function of the tricuspid valve, which separates the right atrium from the right ventricle. This condition occurs during fetal development when the valve doesn't form properly. As a result, the tricuspid valve is positioned lower than normal, causing blood to leak back into the right atrium.
While the exact cause of Ebstein's anomaly is unknown, researchers believe that genetic factors and certain medications taken during pregnancy may play a role. This condition is typically diagnosed during infancy or childhood, although some cases may go unnoticed until adulthood.
Here are some key facts about Ebstein's anomaly:
Living with Ebstein's anomaly requires ongoing care and monitoring. Individuals with this condition should work closely with a healthcare team specialized in congenital heart defects to manage their symptoms and maintain a good quality of life.
In conclusion, Ebstein's anomaly is a rare congenital heart defect that affects the tricuspid valve. Early diagnosis and appropriate medical management are crucial for individuals with this condition. Regular follow-up and adherence to treatment plans can help minimize complications and improve overall well-being.
Ebstein's anomaly is a rare congenital heart defect that affects the tricuspid valve, the valve that separates the right atrium and the right ventricle. This condition can lead to abnormal blood flow and can cause various symptoms, including shortness of breath, fatigue, and heart palpitations. Treatment options for Ebstein's anomaly depend o...
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